@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_head {
  this: np:hasAssertion dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion;
    np:hasProvenance dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance;
    np:hasPublicationInfo dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion a np:Assertion .
  
  dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance a np:Provenance .
  
  dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion {
  miriam-gene:2571 a ncit:C16612 .
  
  lld:C0600327 a ncit:C7057 .
  
  dgn-gda:DGNf793fae67b411e8575d37bb38d7fc4e7 sio:SIO_000628 miriam-gene:2571, lld:C0600327;
    a sio:SIO_001121 .
}

dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance {
  dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion dcterms:description
      "[The GAD1-TSS(-50kbLoop) was enriched with nucleosomes epigenetically decorated with the transcriptional mark, histone H3 trimethylated at lysine 4, and was weak or absent in skin fibroblasts and pluripotent stem cells compared with neuronal cultures differentiated from them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:23864674;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:46+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}